The Recall Desk

State

American Samoa product recalls

73,570 recalls have nationwide distribution and so reach American Samoa. 25 additional recalls listed American Samoa specifically in their distribution scope.

What the numbers show

Total
25
Critical
1
Severe
9
Most recent
2026-09-09

Of the 25 recalls naming American Samoa we have scored against our rubric, 1 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 9 (36%) are Severe.

Which agencies issued them

These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26876–26900 of 73595

  • SevereNHTSA·20E086000·2020-11-16

    Aries Recalls Tow Hitches Due to Potential Structural Failure

    Aries Industries is recalling certain Class 3 and Class 4 tow hitches because they may not support rated weights, risking hitch failure and vehicle separation.

    Product
    TRAILER HITCHES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V706000·2020-11-16

    2021 Motorhomes Recalled for Bed Lift Motor Failure and Collapse Risk

    REV Recreation Group is recalling certain 2021 motorhomes (Fleetwood and Holiday Rambler models) because the primary gear in the bed lift motor may fail, allowing the bed frame to drop and increase injury risk.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD NAVIGATOR, NAUTICA, ENDEAVOR, ARMADA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-11152020-01·2020-11-15

    Tucson Tamale Wholesale Recalls Chicken and Pork Tamales Due to Plastic Contamination

    Tucson Tamale Wholesale Company LLC is recalling frozen chicken and pork tamales because they may contain hard plastic from diced tomatoes in puree.

    Product
    Tucson Tamale Wholesale Company LLC — FSIS Issues Public Health Alert for Chicken and Pork Tamales Containing FDA-Regulated Diced Tomatoes in Puree That Have Been Recalled Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V704000·2020-11-13

    Zero Motorcycles Recalls 2020 SR/F and SR/S Models for Brake Switch Defect

    Zero Motorcycles is recalling 2020 SR/F and SR/S motorcycles because water can enter the front brake switch, preventing the brake light from illuminating and increasing crash risk.

    Product
    ZERO — ZERO SR/F, SR/S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V701000·2020-11-13

    Chevrolet Bolt EV Recalled Due to High Voltage Battery Fire Risk

    General Motors is recalling 2017-2019 Chevrolet Bolt EVs because the high voltage battery could catch fire when charged to full capacity, increasing the risk of injury.

    Product
    CHEVROLET — CHEVROLET BOLT EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V702000·2020-11-13

    2021 Volkswagen Atlas Tires Recalled for Over-Cure Defect

    Volkswagen is recalling certain 2021 Atlas and 2020-2021 Atlas Cross Sport vehicles with potentially over-cured Continental Cross Contact LX Sport tires. Over-cured tires can cause sidewall breaks or tread separation, increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS CROSS SPORT, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V703000·2020-11-13

    2021 Winnebago Motorhomes Recalled for Power Bed Motor Failure Risk

    Certain 2021 Winnebago motorhomes are being recalled because the power bed motor may fail internally, causing the bed to extend before the safety strap engages. This can result in the bed falling unexpectedly, posing a risk of injury or death.

    Product
    WINNEBAGO — WINNEBAGO REVEL, VISTA, ADVENTURER, SUNSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V699000·2020-11-12

    Jeep Grand Cherokee Recalled for EGR Cooler Fire Risk

    Chrysler is recalling 2014-2019 Jeep Grand Cherokee vehicles with 3.0L EcoDiesel engines because a cracked EGR cooler may cause an intake manifold fire.

    Product
    JEEP — JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V700000·2020-11-12

    Fuel tank weld defect may cause fuel leak and fire risk

    BMW and Toyota are recalling certain 2020-2021 Z4 and Supra vehicles due to insufficient fuel tank welds that may cause fuel leaks and increase fire risk. Owners should contact their dealer for a free replacement.

    Product
    TOYOTA — TOYOTA, BMW SUPRA, Z4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V698000·2020-11-12

    2021 Toyota RAV4 Prime headlight aiming caps may improperly adjust

    Certain 2021 Toyota RAV4 Prime vehicles have improperly closed headlight aiming caps that can be adjusted horizontally. This can increase glare and reduce driver visibility, increasing the risk of a crash.

    Product
    TOYOTA — TOYOTA RAV4 PRIME
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21707·2020-11-12

    Zinus Recalls Metal Bunk Beds Due to Fall and Injury Hazards

    Zinus is recalling about 26,000 metal bunk beds because welds on the upper bunk can fail, causing the bed to collapse and posing fall and injury hazards.

    Product
    Zinus metal bunk beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0344-2021·2020-11-11

    Zimmer Biomet Recalls Acetabular Hip Prosthesis Cups Due to Sterilant Concerns

    Zimmer Biomet is recalling 412 acetabular hip prosthesis cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.

    Product
    ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, Neutral, O.D. Cup with Spacers, 55 mm Item Number: 00-8065-552-32
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0338-2021·2020-11-11

    Zimmer Biomet Recalls Acetabular Hip Cups Due to Sterilant Biocompatibility Concerns

    Zimmer Biomet is recalling 412 acetabular hip cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.

    Product
    ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, Neutral, O.D. Cup with Spacers, 53 mm Item Number: 00-8065-550-26
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0373-2021·2020-11-11

    Zimmer Biomet Recalls Acetabular Hip Cup Components Due to Sterilant Concerns

    Zimmer Biomet is recalling 412 acetabular hip cup components because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.

    Product
    ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, 10 degree inclined face, O.D. Cup with Spacers, 53 mm Number: 00-8065-650-28
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0067-2021·2020-11-11

    Nostrum Recalls Metformin Hydrochloride Extended-Release Tablets Due to NDMA Impurity

    Nostrum Laboratories is recalling Metformin Hydrochloride Extended-Release Tablets 750 mg because the NDMA impurity level exceeds acceptable intake limits.

    Product
    Metformin Hydrochloride Extended-Release Tablets, USP 750 mg, 100 count bottles, Rx Only. Manufactured by: Nostrum Laboratories, Inc. Kansas City, MO 64120. NDC 29033-056-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0068-2021·2020-11-11

    Nostrum Recalls Metformin Hydrochloride Extended-Release Tablets Due to NDMA Impurity

    Nostrum Laboratories is recalling 20,872 bottles of Metformin Hydrochloride Extended-Release Tablets 500 mg because they contain N-Nitrosodimethylamine (NDMA) above acceptable levels.

    Product
    Metformin Hydrochloride Extended-Release Tablets, USP 500 mg, 100 count bottles, Rx Only. Manufactured by: Nostrum Laboratories, Inc. Kansas City, MO 64120. NDC 29033-055-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0335-2021·2020-11-11

    Zimmer Biomet Recalls Acetabular Cup Hip Prosthesis Due to Sterilant Concerns

    Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.

    Product
    ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, Neutral, O.D. Cup with Spacers, 51 mm Item Number: 00-8065-548-28
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0062-2021·2020-11-11

    Metformin Hydrochloride Extended Release Tablets Recalled for NDMA Impurity

    Marksans Pharma Limited is recalling Metformin Hydrochloride Extended Release tablets due to N-Nitrosodimethylamine (NDMA) impurity levels above acceptable intake limits.

    Product
    METFORMIN HYDROCHLORIDE EXTENDED RELEASE — METFORMIN HYDROCHLORIDE EXTENDED RELEASE (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0346-2021·2020-11-11

    Zimmer Biomet Recalls Hip Prosthesis Cups Due to Sterilant Biocompatibility Concerns

    Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.

    Product
    ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, Neutral, O.D. Cup with Spacers, 57 mm Number: 00-8065-554-26
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0333-2021·2020-11-11

    Zimmer Biomet Recalls Acetabular Hip Cup Components Due to Sterilant Concerns

    Zimmer Biomet is recalling 412 acetabular hip cup components because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.

    Product
    ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22mm, Neutral, O.D. Cup with Spacers, 51 mm Item Number: 00-8065-548-22
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0056-2021·2020-11-11

    Denton Pharma Recalls Metformin Hydrochloride Tablets Due to NDMA Impurity

    Denton Pharma, Inc. is recalling Metformin Hydrochloride Extended-Release Tablets 750 mg due to the detection of N-Nitrosodimethylamine (NDMA) impurity above acceptable intake levels.

    Product
    Metformin Hydrochloride Extended-Release Tablets USP 750 mg, 30 Tablets bottle, Rx Only, Time-Cap Labs, Inc., Repackaged By: Northwind Pharmaceuticals North Blenheim NY 12131 NDC 70934-334-30
    Category
    Drug
    Distribution
    Distributed nationwide